HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706661Generated: October 26, 2026
2-Morpholinoethanol → 4-(2-Morpholinoethoxy)pyridin-2-amine
https://huagongshe.com/reaction/706661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Morpholinoethanol | HCID 61163 | — |
| Reactant | 2-Amino-4-chloropyridine | HCID 581866 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Morpholinoethoxy)pyridin-2-amine | HCID 67252085 | 69.3% |
Reaction Steps
2-Morpholinoethanol (2.21 g, 16.8 mmol) was treated with sodium (0.407 g, 17.7 mmol) until a homogeneous suspension was obtained. 4-Chloropyridin-2-amine (1.14 g, 8.86 mmol) was added and the mixture was heated with magnetic stirring at 145° C. in a sealed tube for 10 hours. The reaction mixture was cooled and diluted with water and EtOAc. The layers were separated, and the aqueous phase was extracted twice with EtOAc. The combined organic extracts were concentrated to afford a viscous oil which was subjected to chromatographic purification on silica with 10% MeOH/DCM as eluent to provide 1.37 g of desired product as a low-melting solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174981B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4971f8f9cc7e41dfbc954fa9da65ab86 |
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| Source note | uspto-grants-2015_11 |
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